A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212347



Internal ID20779387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73254801..73261600hg38UCSC Ensembl
chr4:74120518..74127317hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384304
Supporting Variants
Samples
Known GenesANKRD17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212347
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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